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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277850Generated: October 26, 2026

Tetrahydrofuran → 6-bromo-2,4-dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazine

https://huagongshe.com/reaction/277850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcetateHCID 8857—
Reactant2-Amino-5-bromobenzophenoneHCID 99677—
ReactantAmmonium SulfateHCID 6097028—
Product6-bromo-2,4-dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazineHCID 2343558270%

Reaction Steps

To a solution of (2-amino-5-bromophenyl)(phenyl)methanone (1 g, 3.6 mmol) in anhydrous THF (15 mL) was added at room temperature under nitrogen methylmagnesium bromide (3M in ether, 3 mL, 9 mmol). After 3 hours, the mixture was treated with a saturated aqueous ammonium sulfate solution (30 mL) and ethyl acetate (50 mL). The organic layer was separated, dried (MgSO4), and evaporated. The residue was then dissolved in anhydrous toluene and treated at ambient temperature under nitrogen with acetylaldehyde (2 mL). After 2 minutes, the solvent was removed and residue was purified by a column chromatography (silica gel, hexane:ethyl acetate/4:1) to afford 6-bromo-2,4-dimethyl-4-phenyl-1,4-dihydro-2H-3,1-benzoxazine as a yellowish solid (0.8 g, 70%): MS (ESI) m/z 318/320 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358948B1
Source datasetuspto-grants-2002_03
ORD IDord-17c8211cb7114634b6ed69e28a18cb2c
Source noteuspto-grants-2002_03